Caulerpenyne blocks MBP kinase activation controlling mitosis in sea urchin eggs

• Published in: European journal of cell biology Vol. 78; no. 12; pp. 903 - 910
• Main Authors: Pesando, Danielle, Pesci-Bardona, Catherine, Huitorel, Philippe, Girard, Jean-Pierre
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.12.1999
• Subjects: Animals; Antineoplastic Agents - pharmacology; Caulerpenyne; Dose-Response Relationship, Drug; Embryo, Nonmammalian - cytology; Embryo, Nonmammalian - physiology; Enzyme Activation - drug effects; Enzyme Inhibitors - pharmacology; Flavonoids - pharmacology; MAP kinase; Mitogen-Activated Protein Kinases - antagonists & inhibitors; Mitogen-Activated Protein Kinases - physiology; mitosis; Mitosis - physiology; sea urchin; Sea Urchins - cytology; Sea Urchins - embryology; Sea Urchins - physiology; Sesquiterpenes - pharmacology; Signal Transduction - drug effects; MAP kinase; sea urchin; mitosis; Caulerpenyne
• ISSN: 0171-9335; 1618-1298
• DOI: 10.1016/S0171-9335(99)80092-2

In a previous study, we demonstrated that caulerpenyne (Cyn), a natural sesquiterpene having an antiproliferative potency, blocked the mitotic cycle of sea urchin embryos at metaphase and inhibited the phosphorylation of several proteins, but did not affect histone H1 kinase activation (Pesando et al, 1998, Eur. J. Cell Biol. 77, 19–26). Here, we show that concentrations of Cyn that blocked the first division of the sea urchin Paracentrotus lividus embryos in a metaphase-like stage (45 µM) also inhibited the stimulation of mitogen-activated protein kinase (MAPK) activity in vivo as measured in treated egg extracts using myelin basic protein (MBP) as a substrate (MBPK). However, Cyn had no effect on MBP phosphorylation when added in vitro to an untreated egg extract taken at the time of metaphase, suggesting that Cyn acts on an upstream activation process. PD 98059 (40 µM), a previously characterized specific syntetic inhibitor of MAPK/extracellular signal-regulated kinase-1 (MEK1), also blocked sea urchin eggs at metaphase in a way very similar to Cyn. Both molecules induced similar inhibitory effects on MBP kinase activation in vivo, but had no direct effect on MBP kinase activity in vitro, whereas they did not affect H1 kinase activation neither in vivo nor in vitro. As a comparison, butyrolactone 1 (100 µM), a known inhibitor of H1 kinase activity, did inhibit H1 kinase of sea urchin eggs in vivo and in vitro, and blocked the sea urchin embryo mitotic cycle much before metaphase. Immunoblots of mitotic extracts, treated with anti-active MAP-kinase antibody, showed that both Cyn and PD 98059 reduced the phosphorylatIon of p42 MAP kinase (Erk2) in vivo.